A Combined Early Cognitive and Physical Rehabilitation Program for People Who Are Critically Ill: The Activity and Cognitive Therapy in the Intensive Care Unit (ACT-ICU) Trial

Author:

Brummel Nathan E.1,Jackson James C.2,Girard Timothy D.3,Pandharipande Pratik P.4,Schiro Elena5,Work Brittany6,Pun Brenda T.7,Boehm Leanne8,Gill Thomas M.9,Ely E. Wesley10

Affiliation:

1. N.E. Brummel, MD, Division of Allergy, Pulmonary, and Critical Care Medicine and Center for Health Services Research, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee. Mailing address: 1211 21st Ave South, Suite 6100, Nashville, TN 37212 (USA).

2. J.C. Jackson, PsyD, Division of Allergy, Pulmonary, and Critical Care Medicine and Center for Health Services Research, Department of Medicine, Vanderbilt University School of Medicine, and Geriatric Research, Education and Clinical Center (GRECC) Service, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee; Department of Psychiatry, Vanderbilt

3. T.D. Girard, MD, MSCI, Division of Allergy, Pulmonary, and Critical Care Medicine, Center for Health Services Research, and Center for Quality of Aging, Department of Medicine, Vanderbilt University School of Medicine, and GRECC Service, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee.

4. P.P. Pandharipande, MD, MSCI, Division of Critical Care, Department of Anesthesiology, Vanderbilt University School of Medicine, and Anesthesia Service, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee.

5. E. Schiro, PT, Acute Rehabilitation Services, Vanderbilt University Medical Center.

6. B. Work, OTR/L, Acute Rehabilitation Services, Vanderbilt University Medical Center.

7. B.T. Pun, RN, MSN, ACNP, Center for Health Services Research, Department of Medicine, Vanderbilt University School of Medicine.

8. L. Boehm, MSN, RN, ACNS-BC, Vanderbilt University School of Nursing, Nashville, Tennessee.

9. T.M. Gill, MD, Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.

10. E.W. Ely, MD, MPH, Division of Allergy, Pulmonary, Critical Care Medicine and Center for Health Services Research, and Center for Quality of Aging, Department of Medicine, Vanderbilt University School of Medicine, and GRECC Service, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee.

Abstract

Background In the coming years, the number of survivors of critical illness is expected to increase. These survivors frequently develop newly acquired physical and cognitive impairments. Long-term cognitive impairment is common following critical illness and has dramatic effects on patients' abilities to function autonomously. Neuromuscular weakness affects similar proportions of patients and leads to equally profound life alterations. As knowledge of these short-term and long-term consequences of critical illness has come to light, interventions to prevent and rehabilitate these devastating consequences have been sought. Physical rehabilitation has been shown to improve functional outcomes in people who are critically ill, but subsequent studies of physical rehabilitation after hospital discharge have not. Post-hospital discharge cognitive rehabilitation is feasible in survivors of critical illness and is commonly used in people with other forms of acquired brain injury. The feasibility of early cognitive therapy in people who are critically ill remains unknown. Objective The purpose of this novel protocol trial will be to determine the feasibility of early and sustained cognitive rehabilitation paired with physical rehabilitation in patients who are critically ill from medical and surgical intensive care units. Design This is a randomized controlled trial. Setting The setting for this trial will be medical and surgical intensive care units of a large tertiary care referral center. Patients The participants will be patients who are critically ill with respiratory failure or shock. Intervention Patients will be randomized to groups receiving usual care, physical rehabilitation, or cognitive rehabilitation plus physical rehabilitation. Twice-daily cognitive rehabilitation sessions will be performed with patients who are noncomatose and will consist of orientation, memory, and attention exercises (eg, forward and reverse digit spans, matrix puzzles, letter-number sequences, pattern recognition). Daily physical rehabilitation sessions will advance patients from passive range of motion exercises through ambulation. Patients with cognitive or physical impairment at discharge will undergo a 12-week, in-home cognitive rehabilitation program. Measurements A battery of neurocognitive and functional outcomes will be measured 3 and 12 months after hospital discharge. Conclusions If feasible, these interventions will lay the groundwork for a larger, multicenter trial to determine their efficacy.

Publisher

Oxford University Press (OUP)

Subject

Physical Therapy, Sports Therapy and Rehabilitation

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